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DOI 10.1016/j.chroma.2018.05.004

Медицинская библиотека · Journal of chromatography. A · 2018

A facile and efficient single-step approach for the fabrication of vancomycin functionalized polymer-based monolith as chiral stationary phase for nano-liquid chromatography.

Xu Dongsheng, Shao Huikai, Luo Rongying, Wang Qiqin, Sánchez-López Elena, Fanali Salvatore, Marina Maria Luisa, Jiang Zhengjin

СтатьяПеревод в очереди

Аннотация

A facile single-step preparation strategy for fabricating vancomycin functionalized organic polymer-based monolith within 100μm fused-silica capillary was developed. The synthetic chiral functional monomer, i.e 2-isocyanatoethyl methacrylate (ICNEML) derivative of vancomycin, was co-polymerized with the cross-linker ethylene dimethacrylate (EDMA) in the presence of methanol and dimethyl sulfoxide as the selected porogens. The co-polymerization conditions were systematically optimized in order to obtain satisfactory column performance. Adequate permeability, stability and column morphology were observed for the optimized poly(ICNEML-vancomycin-co-EDMA) monolith. A series of chiral drugs were evaluated on the monolith in either polar organic-phase or reversed-phase modes. After the optimization of separation conditions, baseline or partial enantioseparation were obtained for series of drugs including thalidomide, colchicine, carteolol, salbutamol, clenbuterol and several other β-blockers. The proposed single-step approach not only resulted in a vancomycin functionalized organic polymer-based monolith with acceptable performance, but also significantly simplified the preparation procedure by reducing time and labor.

Для цитирования: Xu Dongsheng, Shao Huikai, Luo Rongying, Wang Qiqin, Sánchez-López Elena, Fanali Salvatore, Marina Maria Luisa, Jiang Zhengjin. A facile and efficient single-step approach for the fabrication of vancomycin functionalized polymer-based monolith as chiral stationary phase for nano-liquid chromatography.. Journal of chromatography. A. 2018. DOI: 10.1016/j.chroma.2018.05.004.

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